Oromandibular dystonia
Symptom Information:
Symptom ID: | HPO:0012048 | |||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of movement(HPO:0100022) Dystonia(HPO:0001332) Focal dystonia(HPO:0004373) Craniofacial dystonia(HPO:0012179) Oromandibular dystonia(HPO:0012048) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Dystonias(MedDRA:10013985) Oromandibular dystonia(HPO:0012048) |
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Database Frequency: | 7 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant cervical dystonia | (Orphanet:93962) |
Autosomal dominant focal dystonia, DYT7 type | (Orphanet:93963) |
DYSTONIA 24 | (OMIM:615034) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 | (OMIM:615643) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Primary dystonia, DYT13 type | (Orphanet:98807) |
Primary dystonia, DYT6 type | (Orphanet:98806) |